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    Natural Products
    Kadsuric acid 3-methylester
    Kadsuric acid 3-methylester
    Information
    CAS No. 1041070-16-9 Price
    Catalog No.CFN92213Purity>=98%
    Molecular Weight484.7Type of CompoundTriterpenoids
    FormulaC31H48O4Physical DescriptionPowder
    Download COA    MSDS    SDFSimilar structuralComparison (Web)  (SDF)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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    Kadsuric acid 3-methylester

    Kadsuric acid 3-methylester
    Product Name Kadsuric acid 3-methylester
    CAS No.: 1041070-16-9
    Catalog No.: CFN92213
    Molecular Formula: C31H48O4
    Molecular Weight: 484.7 g/mol
    Purity: >=98%
    Type of Compound: Triterpenoids
    Physical Desc.: Powder
    Source: The herbs of Kadsura longipedunculata Finet.et Gagnep
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price:
    Download: COA    MSDS    SDF
    Similar structural: Comparison (Web)  (SDF)
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  • ACS Chem Biol.2019, 14(5):873-881
  • Front Pharmacol.2021, 12:762829.
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  • ACS Pharmacol. Transl. Sci.2022, 5,7,479-490
  • Antioxidants (Basel).2021, 10(8):1300.
  • J Ethnopharmacol.2017, 209:305-316
  • Appl Microbiol Biotechnol.2018, 102(12):5105-5120
  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Triterpenoids Compound Library
  • Biological Activity
    Description: Kadsuric acid 3-methylester is a natural product from Kadsura longipedunculata Finet.et Gagnep.
    Kadsuric acid 3-methylester Description
    Source: The herbs of Kadsura longipedunculata Finet.et Gagnep
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.0631 mL 10.3157 mL 20.6313 mL 41.2626 mL 51.5783 mL
    5 mM 0.4126 mL 2.0631 mL 4.1263 mL 8.2525 mL 10.3157 mL
    10 mM 0.2063 mL 1.0316 mL 2.0631 mL 4.1263 mL 5.1578 mL
    50 mM 0.0413 mL 0.2063 mL 0.4126 mL 0.8253 mL 1.0316 mL
    100 mM 0.0206 mL 0.1032 mL 0.2063 mL 0.4126 mL 0.5158 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Helvetica Chimica Acta, 2010 , 91 (5) :856-861.
    Terpenoids from Two Dicranopteris Species[Reference: WebLink]

    METHODS AND RESULTS:
    Two new compounds, (6S,13S)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,14-dien-13-ol (1) and Kadsuric acid 3-methylester (2), together with nine known compounds, (6S,13E)-6-{[β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}cleroda-3,13-dien-15-ol (3), (6S,13S)-6-[6-O-acetyl-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (4), (6S,13S)-6-{[6-O-β-D-glucopyranosyl-(1→4)-α-L-rhamnopyranosyl]oxy}-13-{[α-L-rhamnopyranosyl-(1→4)-β-D-fucopyranosyl]oxy}cleroda-3,14-diene (5), 15-hydroxydehydroabietic acid (6), 15-hydroxylabd-8(17)-en-19-oic acid (7), junicedric acid (8), (4β)-kaur-16-en-18-oic acid (9), (4β)-16-hydroxykauran-18-oic acid (10), and (4β,16β)-16-hydroxykauran-18-oic acid (11) were isolated from the fronds of Dicranopteris linearis or D. ampla.
    CONCLUSIONS:
    Their structures were established by extensive 1D- and 2D-NMR spectroscopy. Compounds 1 and 3–8 showed no anti-HIV activities.
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